| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65227582-65227901 | Rare:92 | ||||
| chr2:66434805-66435282 | Common:2; Rare:114 | ||||
| chr2:68157456-68157937 | Common:2; Rare:248 | ||||
| chr2:68252187-68252258 | Common:1; Rare:21 | ||||
| chr2:69387154-69387373 | Rare:55; Clinvar:2 | ||||
| chr2:69643616-69643834 | Rare:79 | ||||
| chr2:69829477-69829741 | Common:1; Rare:107 | ||||
| chr2:70086890-70087084 | Common:1; Rare:102 | ||||
| chr2:70087433-70087750 | Rare:124 | ||||
| chr2:70257588-70257726 | Common:2; Rare:12 | ||||
| chr2:70257902-70258177 | Common:1; Rare:89 | ||||
| chr2:70293667-70293886 | Common:3; Rare:69 | ||||
| chr2:71068539-71068654 | Rare:52 | ||||
| chr2:71130220-71130677 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 |